DisGeNET is a knowledge management platform that integrates and standardizes the data of genes and mutations related to diseases from multiple sources. It covers entire range of human disease.
Source | Last Updated |
---|---|
DisGeNET | July 29, 2024 |
Disease ID | Disease Name | Gene Symbol | Gene ID | Gene Name | UniProt ID ▼ |
---|---|---|---|---|---|
C0031046 | Pericarditis | CAT | 847 | catalase | P04040 |
C0035309 | Retinal Diseases | CAT | 847 | catalase | P04040 |
C0004509 | Azoospermia | CAT | 847 | catalase | P04040 |
C0021670 | insulinoma | CAT | 847 | catalase | P04040 |
C0751434 | Classical phenylketonuria | CAT | 847 | catalase | P04040 |
C0019202 | Hepatolenticular Degeneration | CAT | 847 | catalase | P04040 |
C0017636 | Glioblastoma | CAT | 847 | catalase | P04040 |
C0001815 | Primary Myelofibrosis | CAT | 847 | catalase | P04040 |
C0033575 | Prostatic Diseases | CAT | 847 | catalase | P04040 |
C0004364 | Autoimmune Diseases | CAT | 847 | catalase | P04040 |
C0024623 | Malignant neoplasm of stomach | CAT | 847 | catalase | P04040 |
C1862389 | ATRIAL SEPTAL DEFECT 1 | CAT | 847 | catalase | P04040 |
C0019061 | Hemolytic-Uremic Syndrome | CAT | 847 | catalase | P04040 |
C0206624 | Hepatoblastoma | CAT | 847 | catalase | P04040 |
C0002871 | Anemia | CAT | 847 | catalase | P04040 |
C0917798 | Cerebral Ischemia | CAT | 847 | catalase | P04040 |
C0598608 | Hyperhomocysteinemia | CAT | 847 | catalase | P04040 |
C3714618 | Primary Hyperthyroidism | CAT | 847 | catalase | P04040 |
C0006413 | Burkitt Lymphoma | CAT | 847 | catalase | P04040 |
C0017152 | Gastritis | CAT | 847 | catalase | P04040 |
C0018081 | Gonorrhea | CAT | 847 | catalase | P04040 |
C0032285 | Pneumonia | CAT | 847 | catalase | P04040 |
C4082937 | Necrotizing enterocolitis in fetus OR newborn | CAT | 847 | catalase | P04040 |
C0020550 | Hyperthyroidism | CAT | 847 | catalase | P04040 |
C0043459 | Zellweger Syndrome | CAT | 847 | catalase | P04040 |
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Last updated: August 19, 2024